KML001 Enhances Anticancer Activity of Gemcitabine Against Pancreatic Cancer Cells
- Authors
- Yang, MH[Yang, Moon Hee]; Lee, KT[Lee, Kyu Taek]; Yang, S[Yang, Sera]; Lee, JK[Lee, Jong Kyoon]; Lee, KH[Lee, Kwang Hyuck]; Rhee, JC[Rhee, Jong Chul]
- Issue Date
- Jan-2015
- Publisher
- INT INST ANTICANCER RESEARCH
- Citation
- ANTICANCER RESEARCH, v.35, no.1, pp.183 - 189
- Indexed
- SCIE
SCOPUS
- Journal Title
- ANTICANCER RESEARCH
- Volume
- 35
- Number
- 1
- Start Page
- 183
- End Page
- 189
- URI
- https://scholarworks.bwise.kr/skku/handle/2021.sw.skku/45099
- ISSN
- 0250-7005
- Abstract
- Background/Aim: Gemcitabine is a drug commonly used to treat pancreatic cancer but chemoresistance to it is a common clinical issue. KML001 (sodium meta-arsenite) has demonstrated certain antitumor activity. The objective of the study was to evaluate the influence of KML001 on the anticancer activity of gemcitabine against pancreatic cancer cells. Materials and Methods: Cell proliferation, migration, and invasion were assessed, as well as the expression of nuclear factor-kappa B (NF-kappa B) p65, epidermal growth factor receptor (EGFR), matrix metalloproteinase-2 (MMP2), and vascular endothelial growth factor-C (VEGFC) in pancreatic cancer cells. Results: Treatment with a combination of KML001 and gemcitabine resulted in significant inhibition of cell proliferation, migration, and invasion, and significantly reduced EGFR and MMP2 expression compared to gemcitabine treatment-alone. Conclusion: Combination treatment of gemcitabine and KML001 could be an effective chemotherapeutic treatment for pancreatic cancer.
- Files in This Item
- There are no files associated with this item.
- Appears in
Collections - Medicine > Department of Medicine > 1. Journal Articles
Items in ScholarWorks are protected by copyright, with all rights reserved, unless otherwise indicated.